Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • Boel
    Member
    • Oct 2009
    • 62

    #1

    BFAST + GATK -> strand bias?

    Hi All,

    I have HiSeq exome data, 75 b paired end. I've used bfast to align, which, if I am not mistaking, converts one end to its complement so that both members of a pair are attributed to the same strand, the pos one, in the resulting bam file.

    If this is true it leads to a problem in GATK (when filtering calls), simply that one can not use strand bias tests (they are all highly sign, all reds are on the same strand). Also, this would also create problem in the read position rank tests, as the 'best' end of every other read is annotated as its 'good' end.

    So the question is: Am I missing something, or are the above conclusions correct?
    Also, is there a way to circumvent this?

    Thanks a bunch,
    Boel
  • nilshomer
    Nils Homer
    • Nov 2008
    • 1283

    #2
    With the newest version of BFAST, you can have the input reads on be the opposite strand to properly represent paired end reads. BFAST will not reverse compliment one end, but the conversion to FASTQ may do so (a new "-k" option avoids this).

    What is your input data, FASTQ files?

    You may get more traction at [email protected].

    Comment

    • Boel
      Member
      • Oct 2009
      • 62

      #3
      Originally posted by nilshomer View Post
      With the newest version of BFAST, you can have the input reads on be the opposite strand to properly represent paired end reads. BFAST will not reverse compliment one end, but the conversion to FASTQ may do so (a new "-k" option avoids this).

      What is your input data, FASTQ files?

      You may get more traction at [email protected].
      Thanks.

      I started with qseq files, converted them with the ill2fastq.pl and then aligned with bfast (bfast+bwa-0.6.5). Did not use the -k option.

      Not sure that this does create a bias, thats what I am trying to figure out. Do you know?
      According to sam format all reads are on the same strand as the reference, which might make this a non-issue. But I must say that I am confused right now.

      Comment

      • nilshomer
        Nils Homer
        • Nov 2008
        • 1283

        #4
        The ill2fastq.pl script will reverse compliment one of the ends, so they are mapped onto the same strand. You can try with the newest release and the "-k" option, as well as supplying the proper pairing information (there is a new "postprocess" pairing option).

        Comment

        • Boel
          Member
          • Oct 2009
          • 62

          #5
          Originally posted by nilshomer View Post
          The ill2fastq.pl script will reverse compliment one of the ends, so they are mapped onto the same strand. You can try with the newest release and the "-k" option, as well as supplying the proper pairing information (there is a new "postprocess" pairing option).
          I am correct in assuming that using bfast in the way I have does create a bias?

          Further, when looking at my reads in IGV most (70%) have a insert size that is positive, while my correct mean insert size should be around -12 (overlapping). Does this suggest that something has gone wrong in the mapping?

          Comment

          • nilshomer
            Nils Homer
            • Nov 2008
            • 1283

            #6
            Originally posted by Boel View Post
            I am correct in assuming that using bfast in the way I have does create a bias?

            Further, when looking at my reads in IGV most (70%) have a insert size that is positive, while my correct mean insert size should be around -12 (overlapping). Does this suggest that something has gone wrong in the mapping?
            Not sure as I don't have enough information. I have tried mapping with pairs that should have a mean insert of zero without problems. Please try the newest version of BFAST and post your results as well as enough information for us to debug.

            Comment

            Latest Articles

            Collapse

            • SEQadmin2
              Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
              by SEQadmin2



              Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

              Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
              ...
              10-14-2026, 09:55 AM
            • SEQadmin2
              New Genomics Technologies Take Aim at Long-Standing Limits
              by SEQadmin2


              Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

              We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
              ...
              09-28-2026, 10:25 AM

            ad_right_rmr

            Collapse

            News

            Collapse

            Topics Statistics Last Post
            Started by SEQadmin2, 10-22-2026, 11:13 AM
            0 responses
            23 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-22-2026, 10:48 AM
            0 responses
            20 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-15-2026, 10:52 AM
            0 responses
            36 views
            0 reactions
            Last Post SEQadmin2  
            Started by SEQadmin2, 10-14-2026, 05:39 AM
            0 responses
            42 views
            0 reactions
            Last Post SEQadmin2  
            Working...